507 related articles for article (PubMed ID: 16672343)
1. A beta1,4-galactosyltransferase is required for Bmp2-dependent patterning of the dorsoventral axis during zebrafish embryogenesis.
Machingo QJ; Fritz A; Shur BD
Development; 2006 Jun; 133(11):2233-41. PubMed ID: 16672343
[TBL] [Abstract][Full Text] [Related]
2. Cloning and genetic mapping of zebrafish BMP-2.
Lee KH; Marden JJ; Thompson MS; MacLennan H; Kishimoto Y; Pratt SJ; Schulte-Merker S; Hammerschmidt M; Johnson SL; Postlethwaite JH; Beier DC; Zon LI
Dev Genet; 1998; 23(2):97-103. PubMed ID: 9770266
[TBL] [Abstract][Full Text] [Related]
3. Fgf signalling controls the dorsoventral patterning of the zebrafish embryo.
Fürthauer M; Van Celst J; Thisse C; Thisse B
Development; 2004 Jun; 131(12):2853-64. PubMed ID: 15151985
[TBL] [Abstract][Full Text] [Related]
4. Differential regulation of chordin expression domains in mutant zebrafish.
Miller-Bertoglio VE; Fisher S; Sánchez A; Mullins MC; Halpern ME
Dev Biol; 1997 Dec; 192(2):537-50. PubMed ID: 9441687
[TBL] [Abstract][Full Text] [Related]
5. bmp1 and mini fin are functionally redundant in regulating formation of the zebrafish dorsoventral axis.
Jasuja R; Voss N; Ge G; Hoffman GG; Lyman-Gingerich J; Pelegri F; Greenspan DS
Mech Dev; 2006 Jul; 123(7):548-58. PubMed ID: 16824737
[TBL] [Abstract][Full Text] [Related]
6. FGF signaling is required for {beta}-catenin-mediated induction of the zebrafish organizer.
Maegawa S; Varga M; Weinberg ES
Development; 2006 Aug; 133(16):3265-76. PubMed ID: 16873584
[TBL] [Abstract][Full Text] [Related]
7. Functional and hierarchical interactions among zebrafish vox/vent homeobox genes.
Gilardelli CN; Pozzoli O; Sordino P; Matassi G; Cotelli F
Dev Dyn; 2004 Jul; 230(3):494-508. PubMed ID: 15188434
[TBL] [Abstract][Full Text] [Related]
8. Maternal and zygotic activity of the zebrafish ogon locus antagonizes BMP signaling.
Miller-Bertoglio V; Carmany-Rampey A; Fürthauer M; Gonzalez EM; Thisse C; Thisse B; Halpern ME; Solnica-Krezel L
Dev Biol; 1999 Oct; 214(1):72-86. PubMed ID: 10491258
[TBL] [Abstract][Full Text] [Related]
9. Asymmetric expression of the BMP antagonists chordin and gremlin in the sea anemone Nematostella vectensis: implications for the evolution of axial patterning.
Rentzsch F; Anton R; Saina M; Hammerschmidt M; Holstein TW; Technau U
Dev Biol; 2006 Aug; 296(2):375-87. PubMed ID: 16828077
[TBL] [Abstract][Full Text] [Related]
10. Heparan sulfate proteoglycans including syndecan-3 modulate BMP activity during limb cartilage differentiation.
Fisher MC; Li Y; Seghatoleslami MR; Dealy CN; Kosher RA
Matrix Biol; 2006 Jan; 25(1):27-39. PubMed ID: 16226436
[TBL] [Abstract][Full Text] [Related]
11. A beta1,4-galactosyltransferase is required for convergent extension movements in zebrafish.
Machingo QJ; Fritz A; Shur BD
Dev Biol; 2006 Sep; 297(2):471-82. PubMed ID: 16904099
[TBL] [Abstract][Full Text] [Related]
12. Three different noggin genes antagonize the activity of bone morphogenetic proteins in the zebrafish embryo.
Fürthauer M; Thisse B; Thisse C
Dev Biol; 1999 Oct; 214(1):181-96. PubMed ID: 10491267
[TBL] [Abstract][Full Text] [Related]
13. Combinatorial Wnt control of zebrafish midbrain-hindbrain boundary formation.
Buckles GR; Thorpe CJ; Ramel MC; Lekven AC
Mech Dev; 2004 May; 121(5):437-47. PubMed ID: 15147762
[TBL] [Abstract][Full Text] [Related]
14. Follistatin and noggin are excluded from the zebrafish organizer.
Bauer H; Meier A; Hild M; Stachel S; Economides A; Hazelett D; Harland RM; Hammerschmidt M
Dev Biol; 1998 Dec; 204(2):488-507. PubMed ID: 9882485
[TBL] [Abstract][Full Text] [Related]
15. Short- and long-range functions of Goosecoid in zebrafish axis formation are independent of Chordin, Noggin 1 and Follistatin-like 1b.
Dixon Fox M; Bruce AE
Development; 2009 May; 136(10):1675-85. PubMed ID: 19369398
[TBL] [Abstract][Full Text] [Related]
16. Sustained Bmp signaling is essential for cloaca development in zebrafish.
Pyati UJ; Cooper MS; Davidson AJ; Nechiporuk A; Kimelman D
Development; 2006 Jun; 133(11):2275-84. PubMed ID: 16672335
[TBL] [Abstract][Full Text] [Related]
17. Gelsolin is a dorsalizing factor in zebrafish.
Kanungo J; Kozmik Z; Swamynathan SK; Piatigorsky J
Proc Natl Acad Sci U S A; 2003 Mar; 100(6):3287-92. PubMed ID: 12629212
[TBL] [Abstract][Full Text] [Related]
18. Essential and opposing roles of zebrafish beta-catenins in the formation of dorsal axial structures and neurectoderm.
Bellipanni G; Varga M; Maegawa S; Imai Y; Kelly C; Myers AP; Chu F; Talbot WS; Weinberg ES
Development; 2006 Apr; 133(7):1299-309. PubMed ID: 16510506
[TBL] [Abstract][Full Text] [Related]
19. A role for MKP3 in axial patterning of the zebrafish embryo.
Tsang M; Maegawa S; Kiang A; Habas R; Weinberg E; Dawid IB
Development; 2004 Jun; 131(12):2769-79. PubMed ID: 15142973
[TBL] [Abstract][Full Text] [Related]
20. IGF binding protein 3 exerts its ligand-independent action by antagonizing BMP in zebrafish embryos.
Zhong Y; Lu L; Zhou J; Li Y; Liu Y; Clemmons DR; Duan C
J Cell Sci; 2011 Jun; 124(Pt 11):1925-35. PubMed ID: 21558420
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]